Executive Pharmacovigilance

Role & Responsibilities
• Perform ICSR case processing and safety data entry in Argus Safety Database within defined timelines
• Download, triage, upload, and book-in regulatory and EMA MLM safety reports
• Manage literature screening, case triaging, and safety data archiving
• Ensure accurate MedDRA coding for all reported adverse events
• Follow pharmacovigilance SOPs, processes, and global guidelines strictly
• Communicate safety data requirements with internal and external stakeholders
• Maintain compliance with global pharmacovigilance legislation and reporting timelines
• Support aggregate reporting and signal management activities

Qualification
• Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Biotechnology, or related disciplines

Experience
• 1–3 years of experience in Pharmacovigilance or Drug Safety
• Hands-on experience with ICSR processing and Argus Safety Database preferred

Skills
• Strong knowledge of ICSR workflows, MedDRA coding, and regulatory reporting
• Good understanding of GVP guidelines and global PV regulations
• High attention to detail and quality-focused approach
• Excellent written and verbal communication skills
• Ability to manage multiple tasks and meet strict timelines

About the Company
• Jubilant Pharma Limited is a global integrated pharmaceutical organisation, Operates USFDA-approved manufacturing and research facilities, Engaged in pharmaceuticals, generics, and drug safety operations.